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Fidial Plus

EUDAMED

Class III (EU MDR)

Ref 10001116Model QQD4-01-1A1

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
FIDIAL PLUS EUDAMED
Device Name
FIDIAL PLUS EUDAMED
Model / Reference
QQD4-01-1A1 EUDAMED
10001116 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100011162U EUDAMED
Basic UDI-DI
B-100011162U EUDAMED
EMDN Code
Q02030301 OPHTHALMOLOGY, HYALURONIC ACID AND DERIVATIVES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Fidial Plus by Fidia Farmaceutici S.p.A. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IT-MF-000026988

Sources (1)

  • EUDAMED 1dbdadba-f234-4d3a-b50a-92da81352b21 61 fields · synced Jun 19, 2026